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Nov 20, 2025

Midlothian, VA

|

Customer Service

|

Contract-to-perm

|

$14 - $18 (hourly estimate)

{"JobID":469500,"JobType":["Contract-to-perm"],"EmployerID":null,"Location":{"Latitude":-77.46,"Longitude":37.55,"Distance":null},"State":"Virginia","Zip":"23225","ReferenceID":"RIC-e74a3575-6799-42fa-883c-6fbcbb83c961","PostedDate":"\/Date(1763653606000)\/","Description":"Insight Global is seeking a detail-oriented and professional Customer Service Representative (CSR) to support our pharmaceutical client. This role involves handling client emails and calls, providing professional service, and performing advanced data entry and processing tasks. The ideal candidate will have strong communication skills, a high level of accuracy, and experience working in a regulated environment.Responsibilities: ? Respond promptly and professionally to emails with an occasional phone call from providers and clients and report all conversations and findings.? Accurately log and track all customer interactions in systems and databases.? Process orders and service requests in compliance with company and regulatory standards.? Perform higher-level data entry tasks, including verifying product information, updating records, and generating reports.? Escalate complex issues to appropriate departments while ensuring timely follow-up and resolution.? Maintain up-to-date knowledge of products, services, and compliance requirements.? Collaborate with cross-functional teams including sales, logistics, and regulatory affairs to ensure customer satisfaction.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Customer Service Representative","City":"Midlothian","ExpirationDate":null,"PriorityOrder":0,"Requirements":"? 1-3 years for customer service/liaison/analyst experience.? Experience in banking/finance/analyst/research/data entry roles? Strong communication and writing/typing skills.? Comfortability with repetitive environment and tasks.","Skills":"Excel experience","Industry":"Customer Service","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":18.0000,"SalaryLow":14.4000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Insight Global is seeking a detail-oriented and professional Customer Service Representative (CSR) to support our pharmaceutical client. This role involves handling client emails and calls, providing... professional service, and performing advanced data entry and processing tasks. The ideal candidate will have strong communication skills, a high level of accuracy, and experience working in a regulated environment.Responsibilities: ? Respond promptly and professionally to emails with an occasional phone call from providers and clients and report all conversations and findings.? Accurately log and track all customer interactions in systems and databases.? Process orders and service requests in compliance with company and regulatory standards.? Perform higher-level data entry tasks, including verifying product information, updating records, and generating reports.? Escalate complex issues to appropriate departments while ensuring timely follow-up and resolution.? Maintain up-to-date knowledge of products, services, and compliance requirements.? Collaborate with cross-functional teams including sales, logistics, and regulatory affairs to ensure customer satisfaction.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Jul 27, 2026

Chicago, IL

|

Programmer / Developer

|

Contract

|

$40 - $50 (hourly estimate)

{"JobID":556923,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-87.68,"Longitude":41.83,"Distance":null},"State":"Illinois","Zip":"60661","ReferenceID":"NYC-83ce67cb-98a6-43b0-bded-b4124794abc2","PostedDate":"\/Date(1785176924000)\/","Description":"Insight Global is seeking a Data Engineer to join an enterprise healthcare client focused on a consumer application called Health 100. Join a growing analytics-focused engineering team supporting this multi-year strategic initiative that brings all your healthcare needs and insights to one place. This role will focus on building and scaling data platforms, pipelines, and services that power analytical products for internal and external clients. This application is particularly focused on providing B2B insights, mainly for few a clients in pharmaceutical manufacturing. The environment is fast-paced, growing, and centered around greenfield development efforts. New requirements are continuously being added, fueling the need for additional engineers. This is expected to be a long term, multi-year engagement.Key Responsibilities? Design, build, and maintain cloud-based data pipelines from the ground up.? Develop data processing solutions using Python, SQL, and PySpark.? Execute assigned user stories in sprint cycles and proactively contribute to requests. ? Build scalable data engineering solutions to support analytics and insights use cases.? Work across multiple projects and quickly adapt to new technologies and requirements.? Collaborate with engineers, analysts, and business stakeholders in an agile squad model.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Data Engineer","City":"Chicago","ExpirationDate":null,"PriorityOrder":0,"Requirements":"? 3+ years of professional experience in data engineering.? Strong hands-on expertise with Python and SQL.? Experience designing and building data pipelines from scratch.? Experience with cloud-based data engineering solutions.? Knowledge of workflow orchestration tools such as Airflow or similar technologies.? Experience working in cloud environments such as GCP or other major cloud platforms.? Ability to work independently and own assigned projects in an agile environment.","Skills":"? PySpark.? GCP? Experience supporting API development and data delivery solutions.? Background in analytical or insights-driven data engineering environments.? Experience supporting software or feature development initiatives.? Passion for identifying and building workflow efficiencies with AI technologies.","Industry":"Programmer / Developer","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":50.0000,"SalaryLow":40.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Insight Global is seeking a Data Engineer to join an enterprise healthcare client focused on a consumer application called Health 100. Join a growing analytics-focused engineering team supporting... this multi-year strategic initiative that brings all your healthcare needs and insights to one place. This role will focus on building and scaling data platforms, pipelines, and services that power analytical products for internal and external clients. This application is particularly focused on providing B2B insights, mainly for few a clients in pharmaceutical manufacturing. The environment is fast-paced, growing, and centered around greenfield development efforts. New requirements are continuously being added, fueling the need for additional engineers. This is expected to be a long term, multi-year engagement.Key Responsibilities? Design, build, and maintain cloud-based data pipelines from the ground up.? Develop data processing solutions using Python, SQL, and PySpark.? Execute assigned user stories in sprint cycles and proactively contribute to requests. ? Build scalable data engineering solutions to support analytics and insights use cases.? Work across multiple projects and quickly adapt to new technologies and requirements.? Collaborate with engineers, analysts, and business stakeholders in an agile squad model.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Jul 07, 2026

Stoughton, MA

|

Pharmacy Technician

|

Contract-to-perm

|

$18 - $22 (hourly estimate)

{"JobID":548859,"JobType":["Contract-to-perm"],"EmployerID":null,"Location":{"Latitude":-71.1089,"Longitude":42.1246,"Distance":null},"State":"Massachusetts","Zip":"02072","ReferenceID":"RIC-15a5aaac-9bb4-4c2e-8949-9e0c5a91d758","PostedDate":"\/Date(1783427389000)\/","Description":"Insight Global is looking for Prior Authorization Technicians to work fully remote in support of one of our large healthcare clients. In this role, the individual will support patient care by removing barriers to medication access. This includes working with insurance companies and clinician offices to facilitate medication approvals through prior authorizations, as well as collaborating with patients and various funding sources, such as foundations or pharmaceutical manufacturers, to obtain financial assistance for high-cost copays. The role also involves providing phone support to patients, navigating pharmacy dispensing systems to adjudicate claims, process refills, and promoting medication adherence.Job Duties:? Communicate directly with insurance companies to facilitate medication approvals.? Navigate pharmacy operating systems to input data, adjudicate test claims, and develop action plans for follow-up.? Communicate effectively across databases, electronic medical records, and email systems to document patient concerns, prior authorization status, and financial assistance needs.? Review prescriptions with physicians? offices to ensure optimal patient care.? Maintain complete and accurate records of patient communications.? Assist patients with managing their pharmacy insurance claims.? Collaborate closely with pharmacists and pharmacy liaisons to deliver a coordinated, high-quality patient care experience.? Communicate directly with patients via phone to support medication adherence and compliance.? Research and analyze information to support strategic decision-making.? Manage, organize, and update relevant data within database systems.? Apply observations and recommendations to improve operations, productivity, quality, and customer service standards.? Identify trends, resolve issues, recommend improvements, and implement changes.? Participate actively in process improvement initiatives.? Act as a value-added business partner to stakeholders across the organization.? Protect organizational value by maintaining confidentiality of information.? Maintain professional knowledge by participating in educational opportunities, reading professional publications, and engaging in professional networks and organizations.? Minimal in-state or out-of-state travel may be required.? Perform other duties as assigned. Hourly Pay Range: $20/hr-$22/hr based on experience.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Certified Pharmacy Technician","City":"Stoughton","ExpirationDate":null,"PriorityOrder":0,"Requirements":"We are seeking experienced, state registered pharmacy technicians. If the candidate lives in a state that does not require registration (i.e. Delaware, Hawaii, New York), candidate agrees to obtain a state license withing 6 months of employment and must be nationally certified (PTCB or NHA) at time of hire. In all other cases, PTCB or NHA is highly preferred but not required (must be obtained within 9 months of employment). Should additional licensure need to be obtained, the applicant will commit to obtaining the required licensure within a mutually agreed upon timeframe. Continued employment is contingent upon meeting these requirements.Years of Experience: Required 1+ years as a Pharmacy TechnicianEducation: High school diploma or GED required","Skills":"Good time management skillsStrong collaborator and team playerOrganized problem solverPTCB","Industry":"Pharmacy Technician","Country":"US","Division":"IT","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":22.0000,"SalaryLow":17.6000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Insight Global is looking for Prior Authorization Technicians to work fully remote in support of one of our large healthcare clients. In this role, the individual will support patient care by... removing barriers to medication access. This includes working with insurance companies and clinician offices to facilitate medication approvals through prior authorizations, as well as collaborating with patients and various funding sources, such as foundations or pharmaceutical manufacturers, to obtain financial assistance for high-cost copays. The role also involves providing phone support to patients, navigating pharmacy dispensing systems to adjudicate claims, process refills, and promoting medication adherence.Job Duties:? Communicate directly with insurance companies to facilitate medication approvals.? Navigate pharmacy operating systems to input data, adjudicate test claims, and develop action plans for follow-up.? Communicate effectively across databases, electronic medical records, and email systems to document patient concerns, prior authorization status, and financial assistance needs.? Review prescriptions with physicians? offices to ensure optimal patient care.? Maintain complete and accurate records of patient communications.? Assist patients with managing their pharmacy insurance claims.? Collaborate closely with pharmacists and pharmacy liaisons to deliver a coordinated, high-quality patient care experience.? Communicate directly with patients via phone to support medication adherence and compliance.? Research and analyze information to support strategic decision-making.? Manage, organize, and update relevant data within database systems.? Apply observations and recommendations to improve operations, productivity, quality, and customer service standards.? Identify trends, resolve issues, recommend improvements, and implement changes.? Participate actively in process improvement initiatives.? Act as a value-added business partner to stakeholders across the organization.? Protect organizational value by maintaining confidentiality of information.? Maintain professional knowledge by participating in educational opportunities, reading professional publications, and engaging in professional networks and organizations.? Minimal in-state or out-of-state travel may be required.? Perform other duties as assigned. Hourly Pay Range: $20/hr-$22/hr based on experience.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Dec 04, 2025

Wilmington, DE

|

Desktop Support

|

Contract

|

$16 - $20 (hourly estimate)

{"JobID":473540,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.53,"Longitude":39.73,"Distance":null},"State":"Delaware","Zip":"19803","ReferenceID":"KPD-7ea60f2e-bd13-4b6f-9009-3872175a5260","PostedDate":"\/Date(1764874307000)\/","Description":"A large pharmaceutical client is looking for a level 1.5 Veeva Support team member to join their team. This role provides comprehensive technical support and system management across multiple regulatory and document management platforms. Responsibilities include end-to-end support (L1?L3) for Veeva RIM and Veeva SafetyDocs Vaults, encompassing issue diagnosis, resolution tracking, and proactive monitoring. The position collaborates with BOT development teams to deliver Veeva RIM API endpoints for automation and integration, and contributes to configuring the Veeva RIM Trainings module within the eLMS Quality Suite to ensure streamlined compliance tracking. Acting as the technical point of contact for PleaseReview (both standalone and Veeva-integrated), the role manages user access, configuration, performance optimization, and license administration. Additional duties include setup and maintenance of ISI Toolbox, lifecycle management of Lorenz docuBridge (including user provisioning and licensing), and support for Lorenz iSubmit installation, configuration, and issue resolution to meet submission standards. The role also involves configuring Word Templates for regulatory workflows, installing and troubleshooting iLovePDF and other document processing tools for high-volume submissions, and managing ServiceNow Request and Incident tickets to ensure timely resolution of customer escalations. This is a remote opportunity working EST hours in LATAM.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"INTL - Level 1.5 Support","City":"Wilmington","ExpirationDate":null,"PriorityOrder":0,"Requirements":"?Experience with the life science and healthcare industry.?Knowledge of GxP, 21 CFR Part 11, Annex 11 and validation processes in a regulated environment.?Strong technical skills in configuration, and issue resolution in Windows-based enterprise environments.?Familiarity with ticketing systems (e.g., ServiceNow) and Request/ incident/change management processes. ?Excellent interpersonal skills and the ability to communicate clearly with both technical and non-technical stakeholders.?Ability to work independently and collaboratively across global, cross-functional teams.?Experience with documentation tools and version control systems is a plus.","Skills":"","Industry":"Desktop Support","Country":"US","Division":"IT","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":20.0000,"SalaryLow":16.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

A large pharmaceutical client is looking for a level 1.5 Veeva Support team member to join their team. This role provides comprehensive technical support and system management across multiple... regulatory and document management platforms. Responsibilities include end-to-end support (L1?L3) for Veeva RIM and Veeva SafetyDocs Vaults, encompassing issue diagnosis, resolution tracking, and proactive monitoring. The position collaborates with BOT development teams to deliver Veeva RIM API endpoints for automation and integration, and contributes to configuring the Veeva RIM Trainings module within the eLMS Quality Suite to ensure streamlined compliance tracking. Acting as the technical point of contact for PleaseReview (both standalone and Veeva-integrated), the role manages user access, configuration, performance optimization, and license administration. Additional duties include setup and maintenance of ISI Toolbox, lifecycle management of Lorenz docuBridge (including user provisioning and licensing), and support for Lorenz iSubmit installation, configuration, and issue resolution to meet submission standards. The role also involves configuring Word Templates for regulatory workflows, installing and troubleshooting iLovePDF and other document processing tools for high-volume submissions, and managing ServiceNow Request and Incident tickets to ensure timely resolution of customer escalations. This is a remote opportunity working EST hours in LATAM.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

May 20, 2026

Upper Providence, PA

|

Engineering (Non IT)

|

Contract

|

$46 - $58 (hourly estimate)

{"JobID":532553,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.45,"Longitude":40.18,"Distance":null},"State":"Pennsylvania","Zip":"19426","ReferenceID":"PHL-eeb22244-ef8f-43c6-9998-3bb32820fba7","PostedDate":"\/Date(1779303862000)\/","Description":"One of our large Pharmaceutical clients is seeking a Data Steward to join them for their growing project work. As a member of the centralized Research Data Standards \u0026 Governance team, the Research Data Steward holds the responsibility for managing the end-to-end lifecycle of research data operational activities by establishing and maintaining data standards and governance practices, to ensure data quality, accuracy, retention, security and compliance with regulatory requirements.This role supports a lab in an automated loop program by driving data stewardship and (potentially) data ownership across research (non-clinical and clinical) datasets?focused primarily on public and externally sourced data. The consultant will establish and promote data standards (ontologies, vocabularies, metadata), enable consistent modeling and integration of internal and purchased/public datasets, and oversee governance that helps multiple research ?tech builds? scale safely and consistently (e.g., multi-omics, sample/asset metadata, and research data warehousing).Key Responsibilities? Serve as a data steward (and potentially a data owner) for causal biology / target identification research datasets, ensuring data is well-defined, governed, and usable across the organization (this is not a clinical data role).? Define, standardize, and promote controlled vocabularies, ontologies, and data standards for research and multi-omics datasets (e.g., genetics, transcriptomics / gene expression, and related omics domains).? Support integration and analysis readiness of external datasets (including biobank data) alongside internal data sources.? Partner with scientists, data product teams, and platform stakeholders to align what is captured for samples vs. omics experiments and ensure consistent linking of assets and metadata.? Contribute to data modeling efforts and standardization that support downstream visualization and reporting tools.? Drive stakeholder engagement and influence: communicate standards clearly, advocate for adoption, and coordinate across teams to reduce fragmentation and improve consistency.? Support multiple research ?tech builds? by defining governance, metadata, and standards that enable consistent capture and reuse across projects (e.g., large molecule design initiatives, lab equipment data pipelines, and sample management/collection: what samples are, how they are used, and how they are traced).? Enable research data capture and storage for cell lines, organoids, and related model systems, including guidance for how to attribute patient populations/indications to molecular models of disease and how to store associated molecular/omics data.? Support scaling of perturbation datasets by helping build and govern a large warehouse of collected data, ensuring consistent structure, metadata, lineage, and quality controls.? Oversee public/external data management, including intake of purchased/partnered public datasets, documentation of provenance, and alignment to internal standards.? Define and operationalize guidance for data terms of use (licenses, permitted use, sharing restrictions, retention) and set/communicate policy expectations for research teams consuming public data.? Classify datasets and use-cases into high / medium / low risk categories and ensure appropriate governance controls are in place (e.g., access expectations, review steps, and documentation).We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Data Steward","City":"Upper Providence","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- Bachelor?s degree or higher in Biology, Bioinformatics, Computational Biology, Data Science (with strong life-sciences focus), or a related field.-Experience working with a LIMS, ELN, or laboratory automation platform (benchling is preferred)-Understands laboratory-generated data and how it moves into computational platforms-Brings knowledge of research laboratory systems and integrated laboratory-to-compute workflows- Hands-on experience with data stewardship and/or data governance concepts (e.g., stewardship operating model, data quality, metadata, ownership, and standards).- Experience working with data standards, ontologies, vocabularies, or controlled terminologies in a research or life-sciences setting.- Knowledge of cloud platforms, specifically google cloud- Understanding of multi-omics data types and workflows (e.g., genetics, transcriptomics/gene expression) and how sample/assay metadata ties to experimental outputs.- Working knowledge of data modeling and structuring datasets for analysis and reuse.","Skills":"- Familiarity and/or experience with concepts related to interoperability, cloud storage platforms and creating integrated data assets from internal generated and externally purchased data.- Knowledge of data privacy laws and regulations is a plus, contributing to compliance and best practices in data stewardship.","Industry":"Engineering (Non IT)","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":58.0000,"SalaryLow":46.4000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

One of our large Pharmaceutical clients is seeking a Data Steward to join them for their growing project work. As a member of the centralized Research Data Standards & Governance team, the Research... Data Steward holds the responsibility for managing the end-to-end lifecycle of research data operational activities by establishing and maintaining data standards and governance practices, to ensure data quality, accuracy, retention, security and compliance with regulatory requirements.This role supports a lab in an automated loop program by driving data stewardship and (potentially) data ownership across research (non-clinical and clinical) datasets?focused primarily on public and externally sourced data. The consultant will establish and promote data standards (ontologies, vocabularies, metadata), enable consistent modeling and integration of internal and purchased/public datasets, and oversee governance that helps multiple research ?tech builds? scale safely and consistently (e.g., multi-omics, sample/asset metadata, and research data warehousing).Key Responsibilities? Serve as a data steward (and potentially a data owner) for causal biology / target identification research datasets, ensuring data is well-defined, governed, and usable across the organization (this is not a clinical data role).? Define, standardize, and promote controlled vocabularies, ontologies, and data standards for research and multi-omics datasets (e.g., genetics, transcriptomics / gene expression, and related omics domains).? Support integration and analysis readiness of external datasets (including biobank data) alongside internal data sources.? Partner with scientists, data product teams, and platform stakeholders to align what is captured for samples vs. omics experiments and ensure consistent linking of assets and metadata.? Contribute to data modeling efforts and standardization that support downstream visualization and reporting tools.? Drive stakeholder engagement and influence: communicate standards clearly, advocate for adoption, and coordinate across teams to reduce fragmentation and improve consistency.? Support multiple research ?tech builds? by defining governance, metadata, and standards that enable consistent capture and reuse across projects (e.g., large molecule design initiatives, lab equipment data pipelines, and sample management/collection: what samples are, how they are used, and how they are traced).? Enable research data capture and storage for cell lines, organoids, and related model systems, including guidance for how to attribute patient populations/indications to molecular models of disease and how to store associated molecular/omics data.? Support scaling of perturbation datasets by helping build and govern a large warehouse of collected data, ensuring consistent structure, metadata, lineage, and quality controls.? Oversee public/external data management, including intake of purchased/partnered public datasets, documentation of provenance, and alignment to internal standards.? Define and operationalize guidance for data terms of use (licenses, permitted use, sharing restrictions, retention) and set/communicate policy expectations for research teams consuming public data.? Classify datasets and use-cases into high / medium / low risk categories and ensure appropriate governance controls are in place (e.g., access expectations, review steps, and documentation).We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Jul 02, 2025

Wilmington, NC

|

Medical Writer

|

Contract

|

$17 - $21 (hourly estimate)

{"JobID":424714,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-77.91,"Longitude":34.21,"Distance":null},"State":"North Carolina","Zip":"28401","ReferenceID":"PHL-f3ce624e-8cb0-4ff4-a605-c5571d4cb8c6","PostedDate":"\/Date(1751484580000)\/","Description":"Our digital advertising client is looking to hire a Copyeditor in LATAM to service their clients. They will be responsible for the basics of copyediting including: performing thorough grammar and spelling checks, review all copy for clarity and logical flow, using a multi-pass approach to catch different error types. They will also be responsible for content accuracy \u0026 style compliance including; ensuring correct spelling of all brand names, companies, products, places, and personal names. Verifying all dates are correct and match their day of the week (e.g., \"Friday, September 9\"). Applying correct AMA (American Medical Association) style throughout. Additionally will ensure formatting consistency across:oHeadlines, subheads, bullet points, and spacing.oSlide notes (in PowerPoint decks), ensuring relevancy and correctness.?Check employee titles where mentioned; confirm via Microsoft Teams or email if unclear.?Review and resolve formatting issues such as widows, orphans, and bullet alignment.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"INTL IT Copyeditor","City":"Wilmington","ExpirationDate":null,"PriorityOrder":0,"Requirements":"?5+ years of copy editing or proofreading experience.?Experience working on PowerPoint presentations and editorial QA of corporate or healthcare materials.?Excellent command of written English and editorial best practices.?High attention to detail and a methodical approach to reviewing documents.?Ability to work independently and under tight deadlines.?Availability for flexible, quick-turnaround assignments.","Skills":"?Strong knowledge of AMA style guidelines.?Experience working with or for healthcare or pharmaceutical companies.","Industry":"Medical Writer","Country":"US","Division":"IT","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":21.0000,"SalaryLow":16.8000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Our digital advertising client is looking to hire a Copyeditor in LATAM to service their clients. They will be responsible for the basics of copyediting including: performing thorough grammar and... spelling checks, review all copy for clarity and logical flow, using a multi-pass approach to catch different error types. They will also be responsible for content accuracy & style compliance including; ensuring correct spelling of all brand names, companies, products, places, and personal names. Verifying all dates are correct and match their day of the week (e.g., "Friday, September 9"). Applying correct AMA (American Medical Association) style throughout. Additionally will ensure formatting consistency across:oHeadlines, subheads, bullet points, and spacing.oSlide notes (in PowerPoint decks), ensuring relevancy and correctness.?Check employee titles where mentioned; confirm via Microsoft Teams or email if unclear.?Review and resolve formatting issues such as widows, orphans, and bullet alignment.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Jul 30, 2026

Irvine, CA

|

Administrative Assistant

|

Contract

|

$38 - $48 (hourly estimate)

{"JobID":558796,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-117.73,"Longitude":33.67,"Distance":null},"State":"California","Zip":"92618","ReferenceID":"OCC-bf34aef8-8994-4c7d-a906-22b120eebc64","PostedDate":"\/Date(1785453279000)\/","Description":"A large medical device company in Irvine, CA is looking for a Clinical Research Specialist. This candidate will play a crucial role in supporting a 10 year post market clinical trial for breast implants. Their key responsibilities will include monitoring clinical studies, data verification, regulatory compliance, study documentation, site visits and coordination, and developing written travel reports.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Clinical Research Specialist","City":"Irvine","ExpirationDate":null,"PriorityOrder":0,"Requirements":"3+ years of experience as a clinical research specialist/associate or field monitor coming from a background of a large research institution, a sponsor company(medical device / biotechnology / pharmaceutical company) , or a hospital3+ years of experience working on a clinical trial Bachelor\u0027s DegreeTravel 25%","Skills":"Experience with Class III medical deviceExperience co monitoring / co shadowing a CROExperience with vendor managementExperience with research na?ve sitesExperience with long term study retention of subjects","Industry":"Administrative Assistant","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":48.0000,"SalaryLow":38.4000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

A large medical device company in Irvine, CA is looking for a Clinical Research Specialist. This candidate will play a crucial role in supporting a 10 year post market clinical trial for breast... implants. Their key responsibilities will include monitoring clinical studies, data verification, regulatory compliance, study documentation, site visits and coordination, and developing written travel reports.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Jun 26, 2026

Danvers, MA

|

Engineering (Non IT)

|

Contract

|

$16 - $20 (hourly estimate)

{"JobID":546184,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-70.9455,"Longitude":42.5694,"Distance":null},"State":"Massachusetts","Zip":"01923","ReferenceID":"BOS-bd69e0f9-9efd-45ca-b910-e1f60d36c776","PostedDate":"\/Date(1782506163000)\/","Description":"Insight Global is seeking a Project Manager to support our Medical Device client. This consultant will sit remotely in Mexico and should have experience in a medical device environment, ideally supporting Quality Systems?related initiatives. This role will manage multiple, overlapping projects and work closely with senior stakeholders to drive execution and visibility. Day to day will consist of the following: Responsibilities-Manage multiple concurrent projects within a regulated medical device environment-Coordinate and communicate with senior-level stakeholders across teams-Develop and maintain project plans, timelines, and status updates-Prepare and coordinate slides, decks, and executive-ready presentations-Track risks, dependencies, and deliverables across initiativesCompensation: $16/hr to $20/hr. Exact compensation may vary based on several factors, including skills, experience, and educationWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"COPY - Project Manager (INTL - Mexico)","City":"Danvers","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-6-8+ years of project management experience within a medical device or regulated life sciences company-Exposure to Quality Systems initiatives or programs-Strong stakeholder management and communication skills-Ability to manage competing priorities in a fast-paced environment-Ability to manage training workflows and documentation in a regulated environment.-Excellent attention to detail, organizational skills, and ability to meet strict deadlines.-Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).-Experience with ComplianceWire is a plus, not required","Skills":"-Prior experience in medical device or pharmaceutical industry.-Familiarity with Windchill or other document management systems.-Experience supporting audit remediation projects (FDA, EU MDR, etc.).-Knowledge of Good Documentation Practices (GDP).","Industry":"Engineering (Non IT)","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":20.0000,"SalaryLow":16.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Insight Global is seeking a Project Manager to support our Medical Device client. This consultant will sit remotely in Mexico and should have experience in a medical device environment, ideally... supporting Quality Systems?related initiatives. This role will manage multiple, overlapping projects and work closely with senior stakeholders to drive execution and visibility. Day to day will consist of the following: Responsibilities-Manage multiple concurrent projects within a regulated medical device environment-Coordinate and communicate with senior-level stakeholders across teams-Develop and maintain project plans, timelines, and status updates-Prepare and coordinate slides, decks, and executive-ready presentations-Track risks, dependencies, and deliverables across initiativesCompensation: $16/hr to $20/hr. Exact compensation may vary based on several factors, including skills, experience, and educationWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Aug 03, 2026

New Brunswick, NJ

|

Business Analyst (BA)

|

Contract

|

$68 - $85 (hourly estimate)

{"JobID":559698,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-74.4494,"Longitude":40.4878,"Distance":null},"State":"New Jersey","Zip":"08901","ReferenceID":"NNJ-a497f391-ed97-4495-bccd-51c3d1c8b3ad","PostedDate":"\/Date(1785789945000)\/","Description":"Insight Global is hiring an NGM Pas-X Business Analyst to support Pas-X MES initiatives for one of its largest clients in the life sciences industry. In this role, you will be responsible for translating business needs into actionable requirements, coordinating deployments, maintaining compliant SDLC documentation, supporting testing and validation, and acting as a liaison between J\u0026J, Koerber/KPS, site teams, Quality, IT, and delivery partners.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"NGM Pas-X Program Business Analyst","City":"New Brunswick","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- Strong Business Analyst, Product, MES, or validation experience in a regulated manufacturing, pharmaceutical, or life sciences environment.- Strong working knowledge of SDLC, GxP/GDP, CSV/validation practices, agile delivery, traceability, and quality control system changes.- Experience using Jira, Confluence, qTest, Microsoft 365, and enterprise change tools.Must have strong communication skills and be able to explain system changes to site teams, Quality, IT, vendors, and business stakeholders.","Skills":"- Korber Pas-X MES knowledge.- Pas-X deployment experience.- Performance testing coordination.- Global curriculum/SOP ownership.- GenAI or digital transformation program support.","Industry":"Business Analyst (BA)","Country":"US","Division":"IT","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":85.0000,"SalaryLow":68.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Insight Global is hiring an NGM Pas-X Business Analyst to support Pas-X MES initiatives for one of its largest clients in the life sciences industry. In this role, you will be responsible for... translating business needs into actionable requirements, coordinating deployments, maintaining compliant SDLC documentation, supporting testing and validation, and acting as a liaison between J&J, Koerber/KPS, site teams, Quality, IT, and delivery partners.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Jul 29, 2026

Wilmington, DE

|

Business Analyst (BA)

|

Contract

|

$48 - $60 (hourly estimate)

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We are seeking an IT Research Support Lead responsible for the operational performance, reliability, and compliance of scientific applications supporting Preclinical and Translational Research. Acts... as the primary IT owner and escalation point for laboratory systems, ensuring applications are stable, audit-ready, and aligned with research workflows. Partners with scientists, QA, infrastructure, cybersecurity, and vendors to deliver application support, manage projects and upgrades, oversee compliance activities, and drive continuous service improvement.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

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